Evidence map›Paper›PMID 31089208›Full record

ArticleBritish journal of cancer2019

The anaphase-promoting complex/cyclosome: a new promising target in diffuse large B-cell lymphoma and mantle cell lymphoma.

Anke Maes, Ken Maes, Hendrik De Raeve, Eva De Smedt, Philip Vlummens, Vanessa Szablewski, Julie Devin, Sylvia Faict, Kim De Veirman, Eline Menu and 6 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  3. Journal of medicinal chemistry · 2025
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  7. Review
  8. Review
  9. Article
  10. Connection Between CDC20 Expression and Hepatocellular Carcinoma Prognosis.Medical science monitor : international medical journal of experimental and clinical research · 2021
    Article
  11. Review
  12. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 6 institutions in 3 countries.

Anke MaesDepartment of Hematology and Immunology, Myeloma Center Brussels, Vrije Universiteit Brussel, Brussels, Belgium.
Ken MaesDepartment of Hematology and Immunology, Myeloma Center Brussels, Vrije Universiteit Brussel, Brussels, Belgium.
Hendrik De RaeveDepartment of Pathology, UZ Brussel, Vrije Universiteit Brussel, Brussels, Belgium.
Eva De SmedtDepartment of Hematology and Immunology, Myeloma Center Brussels, Vrije Universiteit Brussel, Brussels, Belgium.
Philip VlummensDepartment of Hematology and Immunology, Myeloma Center Brussels, Vrije Universiteit Brussel, Brussels, Belgium.
Vanessa SzablewskiDepartment of Biopathology, CHU Montpellier, Montpellier, France.
Julie DevinLaboratory for Monitoring Innovative Therapies, Institute of Human Genetics, CNRS, Montpellier, France.
Sylvia FaictDepartment of Hematology and Immunology, Myeloma Center Brussels, Vrije Universiteit Brussel, Brussels, Belgium.
Kim De VeirmanDepartment of Hematology and Immunology, Myeloma Center Brussels, Vrije Universiteit Brussel, Brussels, Belgium.
Eline MenuDepartment of Hematology and Immunology, Myeloma Center Brussels, Vrije Universiteit Brussel, Brussels, Belgium.
Fritz OffnerHematology, Department of Internal Medicine, Ghent University Hospital, Ghent, Belgium.
Marcel SpaargarenDepartment of Pathology, Lymphoma and Myeloma Center Amsterdam (LYMMCARE), Cancer Center Amsterdam, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
Jérôme MoreauxLaboratory for Monitoring Innovative Therapies, Institute of Human Genetics, CNRS, Montpellier, France.
Karin VanderkerkenDepartment of Hematology and Immunology, Myeloma Center Brussels, Vrije Universiteit Brussel, Brussels, Belgium.
Els Van ValckenborghDepartment of Hematology and Immunology, Myeloma Center Brussels, Vrije Universiteit Brussel, Brussels, Belgium.
Elke De BruyneDepartment of Hematology and Immunology, Myeloma Center Brussels, Vrije Universiteit Brussel, Brussels, Belgium. Elke.De.Bruyne@vub.be.
Vrije Universiteit Brussel · BEGhent University Hospital · BEAmsterdam University Medical Centers · NLCentre Hospitalier Universitaire de Montpellier · FRCentre National de la Recherche Scientifique · FRInstitut de Génétique Humaine · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aggressive B-cell non-Hodgkin lymphomas diffuse large B-cell lymphoma (DLBCL) and mantle cell lymphoma (MCL) are characterised by a high proliferation rate. The anaphase-promoting complex/cyclosome (APC/C) and its co-activators Cdc20 and Cdh1 represent an important checkpoint in mitosis. Here, the role of the APC/C and its co-activators is examined in DLBCL and MCL.

methodsThe expression and prognostic value of Cdc20 and Cdh1 was investigated using GEP data and immunohistochemistry. Moreover, the therapeutic potential of APC/C targeting was evaluated using the small-molecule inhibitor proTAME and the underlying mechanisms of action were investigated by western blot.

resultsWe demonstrated that Cdc20 is highly expressed in DLBCL and aggressive MCL, correlating with a poor prognosis in DLBCL. ProTAME induced a prolonged metaphase, resulting in accumulation of the APC/C-Cdc20 substrate cyclin B1, inactivation/degradation of Bcl-2 and Bcl-xL and caspase-dependent apoptosis. In addition, proTAME strongly enhanced the anti-lymphoma effect of the clinically relevant agents doxorubicin and venetoclax.

conclusionWe identified for the first time APC/C as a new, promising target in DLBCL and MCL. Moreover, we provide evidence that Cdc20 might be a novel, independent prognostic factor in DLBCL and MCL.

Indexed as

Anaphase-Promoting Complex-CyclosomeAntigens, CDApoptosisCadherinsCdc20 ProteinsCell Line, TumorGene Expression ProfilingHumansImmunohistochemistryLymphoma, Large B-Cell, DiffuseLymphoma, Mantle-CellMolecular Targeted TherapyProdrugsPrognosisRNA, MessengerTosylarginine Methyl EsterAnaphase-Promoting Complex-CyclosomeAntigens, CDCadherinsCDC20 protein, humanCdc20 ProteinsCDH1 protein, humanProdrugsRNA, MessengerTosylarginine Methyl Ester

Identifiers

PMID31089208
PMCPMC6738099
OpenAlexW2946595518

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.